LINC02997 long intergenic non-protein coding RNA 2997

Information
Symbol
LINC02997
Type
ncRNA
Description
long intergenic non-protein coding RNA 2997
Entrez Gene ID
101928858
Genome
hg19
Position
chr5:66,753,449-67,097,037
Genome
hg38
Position
chr5:67,457,621-67,801,209
HGNC
HGNC:56113 HGNC
Ensembl
ENSG00000249364 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
HGNC HGNC:56113 HGNC
Ensembl ENSG00000249364 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000515227.2 hg38 chr5 67,793,141 67,805,238 12,098
ENST00000668508.1 hg38 chr5 67,457,621 67,801,209 343,589
ENST00000653448.1 hg38 chr5 67,793,163 67,805,236 12,074
ENST00000660391.1 hg38 chr5 67,793,145 67,801,175 8,031
ENST00000659965.1 hg38 chr5 67,763,986 67,805,295 41,310
ENST00000515227.2 hg19 chr5 67,088,969 67,101,066 12,098
ENST00000653448.1 hg19 chr5 67,088,991 67,101,064 12,074
ENST00000659965.1 hg19 chr5 67,059,814 67,101,123 41,310
ENST00000660391.1 hg19 chr5 67,088,973 67,097,003 8,031
ENST00000668508.1 hg19 chr5 66,753,449 67,097,037 343,589
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